Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Water | HCID 962 | — |
| Edukt | P-Xylene | HCID 7809 | — |
| Edukt | 1,3,5-Trihydroxy-1,3,5-triazinane-2,4,6-trione | HCID 10419723 | — |
| Katalysator | Cobalt diacetate | HCID 6277 | — |
| Katalysator | Manganous Acetate | HCID 12525 | — |
| Produkt | Terephthalic Acid | HCID 7489 | 99% |
Reaktionsschritte
In an autoclave, 0.212 g of p-xylene, 0.011 g of hexahydro-1,3,5-trihydroxy-1,3,5-triazine-2,4,6-trione (3% by mole relative to p-xylene), 5 g of acetic acid, 0.003 g of cobalt(II) acetate.4H2O, 0.003 g of manganese(II) acetate.4H2O and 0.001 g of zirconium oxyacetate were placed. The autoclave was charged with 2 MPa of air and placed in a heated oil bath. The mixture was stirred at 150° C. for 12 hours. After the completion of reaction, the autoclave was placed on cold water to cool down the reaction mixture quickly. The resulting mixture was analyzed by high performance liquid chromatography and was found to yield terephthalic acid in 99% yield at 100% conversion of p-xylene.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07091342B2 |
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| Quelldatensatz | uspto-grants-2006_08 |
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| ORD ID | ord-6126e02d02c2469fb6ad8fa1a7eee34a |
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| Quellennotiz | uspto-grants-2006_08 |
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